Health Condition 1: null- Adult ASAPS-I and II patients
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Weight- 40 to 70 kg 2. ASA PS- I and II 3. Patients Undergoing planned surgeries under GA of Duration of 45-120 minutes.
Exclusion criteria
Exclusion criteria: 1.Patients with likely difficult airway 2.Patients with Gastro esophageal reflux disease 3.Patients with full stomach 4.Patients with known allergy to latex 5.Recent history of sore throat or common cold with in last 10 days 6.Patients with acute or chronic cardiovascular diseases, respiratory diseases, renal or liver insufficiency. 7.Patients who consume alcohol and who smoke 8.Patient not willing to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) To compare safety and efficacy of P-LMA versus ETT using ventilatory parameters to assess feasibility of airway device during low flow anaesthesia The parameter comprises of Oropharyngeal leak pressureTimepoint: 1) To compare safety and efficacy of P-LMA versus ETT using ventilatory parameters to assess feasibility of airway device during low flow anaesthesia The parameter comprises of Oropharyngeal leak pressure 5 min after insertion of airway device. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Inspired and Expired tidal volume and their difference 2. Peak / plateau pressure 3. To assess respiratory parameters during low flow anaesthesia a)Inspired and Expired Isoflurane concentration b)Continuous monitoring of ETCO2(iCO2) c)Inspired and expired N2O concentration d)Fraction of inspired oxygen(FiO2) 4.To observe for hemodynamic changes and post-operative complications of both devices if any Timepoint: 1,5,10,20,30,40,50,60,90,120 min | — |
Countries
India
Contacts
Dept. of Anesthesiology, Medical College, Baroda